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	<id>http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Zoernigi</id>
	<title>Organic Chemistry Wiki Spring 2019 - User contributions [en]</title>
	<link rel="self" type="application/atom+xml" href="http://organicchem.sites.grinnell.edu/wiki/spring19/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Zoernigi"/>
	<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/Special:Contributions/Zoernigi"/>
	<updated>2026-11-06T01:00:34Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkane&amp;diff=1459</id>
		<title>Talk:Alkane</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alkane&amp;diff=1459"/>
		<updated>2019-05-10T20:19:52Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: /* Alkane from Wolff-Kischner Reaction (Amelia Zoernig) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Butane (Prof. Swartz) ==&lt;br /&gt;
A reaction of butyl bromide with lithium and then ethanol to form butane.&lt;br /&gt;
&lt;br /&gt;
[[File:Alkane_synthesis.png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Wolff-Kishner Reaction (Alyssa Radakovich) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Wiki_Reaction2.png]]&lt;br /&gt;
&lt;br /&gt;
== Alkane Addition to Benzene (Samuel Alves-Czachor) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkane_addition_to_Benzene_(Samuel_Alves-Czachor).png|1100px]]&lt;br /&gt;
&lt;br /&gt;
== Alkane addition through LDA (Derrick Okine) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Chem_6.png]]&lt;br /&gt;
&lt;br /&gt;
== Grignard Reaction with Functional Group (Alcohol) Removal (Anne Steensma) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Grignard with alcohol removal.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Reduction of Alkenes to Alkanes (Abena Afari) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkane_Synthesis.png|700px]]&lt;br /&gt;
&lt;br /&gt;
== Alkane from Wolff-Kischner Reaction (Amelia Zoernig) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Alkane.JPG]]&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Alkane.JPG&amp;diff=1458</id>
		<title>File:Alkane.JPG</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Alkane.JPG&amp;diff=1458"/>
		<updated>2019-05-10T20:18:36Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=1457</id>
		<title>Talk:Ketone</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=1457"/>
		<updated>2019-05-10T20:14:38Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: /* Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Synthesis of a Ketone from an Acyl Chloride using a Gilman reagent (Nichole Hannan) ==&lt;br /&gt;
&lt;br /&gt;
[[File:KetoneSynthesis.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of ketone from a secondary alcohol (Chloe Wu) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ketone.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Acetic Anhydride and a Grignard Reagent react with an acid workup to produce Acetic Acid and Acetophenone (Malia Wells) ==&lt;br /&gt;
&lt;br /&gt;
[[File:OChem_2_WIKI_Reaction_Ketone.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of ketone from a secondary alcohol (Emily Mamrak) ==&lt;br /&gt;
&lt;br /&gt;
[[File:cyclohexanone.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of 2-butanone from 1-butyne (Madison Howe) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ketone_synthesis.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Electrophilic alkene and soft nucleophile - Klarie Li ==&lt;br /&gt;
&lt;br /&gt;
[[File:Electrophilic_alkene_and_soft_nuclephile.png|600px]]&lt;br /&gt;
&lt;br /&gt;
== Jone&#039;s Oxidation-Steven Sharpe ==&lt;br /&gt;
&lt;br /&gt;
[[File:Jone&#039;s Oxidation.PNG]]&lt;br /&gt;
&lt;br /&gt;
The Jone&#039;s Oxidation provides an easy and relatively cheap way to oxidize an secondary alcohol into a ketone. When a primary alcohol is reduced, it forms a carboxylic acid.&lt;br /&gt;
&lt;br /&gt;
== synthesis of 4-(4-methoxyphenyl)-3-Buten-2-one from 4-methoxy-benzaldehyde and acetone from aldol addition - ( Xuanhe Chen ) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Step2-1.jpg|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of  1-(p-tolyl)propan-2-one  from 1-bromo-4-methylbenzene using Potassium 2-oxopropan-1-ide (Kyle Dixon-Anderson) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Aromatic+ketone synthesis.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Fcaketone.JPG]]&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Fcaketone.JPG&amp;diff=1456</id>
		<title>File:Fcaketone.JPG</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Fcaketone.JPG&amp;diff=1456"/>
		<updated>2019-05-10T20:10:26Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=1455</id>
		<title>Talk:Ketone</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Ketone&amp;diff=1455"/>
		<updated>2019-05-10T20:09:34Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: /* Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Synthesis of a Ketone from an Acyl Chloride using a Gilman reagent (Nichole Hannan) ==&lt;br /&gt;
&lt;br /&gt;
[[File:KetoneSynthesis.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of ketone from a secondary alcohol (Chloe Wu) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ketone.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Acetic Anhydride and a Grignard Reagent react with an acid workup to produce Acetic Acid and Acetophenone (Malia Wells) ==&lt;br /&gt;
&lt;br /&gt;
[[File:OChem_2_WIKI_Reaction_Ketone.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of ketone from a secondary alcohol (Emily Mamrak) ==&lt;br /&gt;
&lt;br /&gt;
[[File:cyclohexanone.png|500px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of 2-butanone from 1-butyne (Madison Howe) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Ketone_synthesis.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Electrophilic alkene and soft nucleophile - Klarie Li ==&lt;br /&gt;
&lt;br /&gt;
[[File:Electrophilic_alkene_and_soft_nuclephile.png|600px]]&lt;br /&gt;
&lt;br /&gt;
== Jone&#039;s Oxidation-Steven Sharpe ==&lt;br /&gt;
&lt;br /&gt;
[[File:Jone&#039;s Oxidation.PNG]]&lt;br /&gt;
&lt;br /&gt;
The Jone&#039;s Oxidation provides an easy and relatively cheap way to oxidize an secondary alcohol into a ketone. When a primary alcohol is reduced, it forms a carboxylic acid.&lt;br /&gt;
&lt;br /&gt;
== synthesis of 4-(4-methoxyphenyl)-3-Buten-2-one from 4-methoxy-benzaldehyde and acetone from aldol addition - ( Xuanhe Chen ) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Step2-1.jpg|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of  1-(p-tolyl)propan-2-one  from 1-bromo-4-methylbenzene using Potassium 2-oxopropan-1-ide (Kyle Dixon-Anderson) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Aromatic+ketone synthesis.jpg]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of Ketone by Fredyl-Craft Acylation (Amelia Zoernig) ==&lt;br /&gt;
&lt;br /&gt;
[[File:fcaketone.jpg]]&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitrile&amp;diff=1318</id>
		<title>Talk:Nitrile</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitrile&amp;diff=1318"/>
		<updated>2019-02-20T03:08:42Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: /* Addition of a Nucleophilic Nitrile to an Alkene (Amelia Zoernig) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Formation of a Nitrile from a Primary Amide Using Thionyl Chloride (Amelia Zoernig) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Nitrile from Amide .png|700px]]&lt;br /&gt;
&lt;br /&gt;
== Azo Compound Formation Via Aromatic Substitution (Matt Lieberman) ==&lt;br /&gt;
&lt;br /&gt;
In this reaction, benzamine&#039;s amine is converted into a diazonium ion after an O=N+ radical adds a nitrogen and removes the hydrogens from the original nitrogen, releasing water in the process and creating a cation. Then, another benzene molecule with an activating, para, ortho directing group such as this methyl group attacks the positively charged diazonium compound and forms a bond with the positive, outermost nitrogen. A proton is lost to reform the conjugation of the attacking benzene ring. This reaction will mainly happen at the para position because of steric hindrance. [[File:Azo_Compound_Formation.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of a nitrile from cyanide and halogenalkane (Tyria Heath) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Nitrile_formation_from_halogenalknane_&amp;amp;_CN.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Addition of a Nucleophilic Nitrile to an Alkene (Amelia Zoernig) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Nitrile_from_Alkene.png|500px]]&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Nitrile_from_Alkene.png&amp;diff=1317</id>
		<title>File:Nitrile from Alkene.png</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Nitrile_from_Alkene.png&amp;diff=1317"/>
		<updated>2019-02-20T03:06:01Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=1316</id>
		<title>Talk:Alcohol</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Alcohol&amp;diff=1316"/>
		<updated>2019-02-20T02:38:06Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: /* ethanal to 1-phenyl ethan-1-ol George Kaslow */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== SN2 Epoxide Opening with Grignard Reagent - Anne Steensma == &lt;br /&gt;
&lt;br /&gt;
[[File:Sn2 epoxide to alcohol.png|800px]]&lt;br /&gt;
&lt;br /&gt;
== ethanal to 1-phenyl ethan-1-ol George Kaslow  ==&lt;br /&gt;
&lt;br /&gt;
[[File:Untitled_Document-1.png|400px]]&lt;br /&gt;
&lt;br /&gt;
== Dihydroxylation of alkene - Klarie Li ==&lt;br /&gt;
&lt;br /&gt;
[[File:Dihydroxylation.png|600px]]&lt;br /&gt;
&lt;br /&gt;
== addition of Grignards to Aldehydes (Tyria Heath) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Addition_of_grignards_to_aldehydes.png|1000px]]&lt;br /&gt;
&lt;br /&gt;
== Synthesis of Bromobutan-2-ol from Butene (Nichole Hannan) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Chem221bralcoholsynthesis.png]]&lt;br /&gt;
&lt;br /&gt;
== Acid catalyzed hydration of alkene - Klarie Li ==&lt;br /&gt;
&lt;br /&gt;
[[File:Acid_Catalyzed_Hydration_of_Alkenes.png|600px]]&lt;br /&gt;
&lt;br /&gt;
== Anti-Markovnikov Hydroboration-Oxidation - Anne Steensma ==&lt;br /&gt;
&lt;br /&gt;
[[File:Hydroboration oxidation corrected.png|1000px]]&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitrile&amp;diff=1259</id>
		<title>Talk:Nitrile</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=Talk:Nitrile&amp;diff=1259"/>
		<updated>2019-01-27T23:30:47Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: /* Formation of a Nitrile from a Primary Amide Using Thionyl Chloride (Amelia Zoernig) */ new section&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;[[Main_Page]]&lt;br /&gt;
__TOC__&lt;br /&gt;
&lt;br /&gt;
== Formation of a Nitrile from a Primary Amide Using Thionyl Chloride (Amelia Zoernig) ==&lt;br /&gt;
&lt;br /&gt;
[[File:Nitrile from Amide .png|700px]]&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
	<entry>
		<id>http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Nitrile_from_Amide_.png&amp;diff=1258</id>
		<title>File:Nitrile from Amide .png</title>
		<link rel="alternate" type="text/html" href="http://organicchem.sites.grinnell.edu/wiki/spring19/index.php?title=File:Nitrile_from_Amide_.png&amp;diff=1258"/>
		<updated>2019-01-27T23:25:56Z</updated>

		<summary type="html">&lt;p&gt;Zoernigi: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Zoernigi</name></author>
	</entry>
</feed>